Literature DB >> 19575641

Conflicting views on the membrane fusion machinery and the fusion pore.

Jakob B Sørensen1.   

Abstract

Fast exocytosis of synaptic vesicles differs from other membrane fusion reactions by being under tight temporal control by the intracellular calcium concentration. This is achieved by subjecting the SNARE-dependent fusion pathway to additional layers of control, both upstream and downstream of the assembly of the fusogenic SNARE-complex. Here, I review conflicting views on the function of the core fusion machinery consisting of the SNAREs, Munc18, complexin, and synaptotagmin. Munc18 controls docking of vesicles to the plasma membrane and initial SNARE-complex assembly, whereas complexin and synaptotagmin cooperate in holding the SNARE complex in an intermediate release-ready or cocked state. Different effects of complexin and synaptotagmin shape the energy landscape for fusion and make final fusion calcium triggered. The final steps are fusion pore formation and expansion, which allow release of the water-soluble vesicle content. The fusion pore remains the most elusive part of the exocytosis pathway, owing to its short lifetime.

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Year:  2009        PMID: 19575641     DOI: 10.1146/annurev.cellbio.24.110707.175239

Source DB:  PubMed          Journal:  Annu Rev Cell Dev Biol        ISSN: 1081-0706            Impact factor:   13.827


  47 in total

1.  Regulation of fusion pore closure and compound exocytosis in neuroendocrine PC12 cells by SCAMP1.

Authors:  Jie Zhang; David Castle
Journal:  Traffic       Date:  2011-02-25       Impact factor: 6.215

Review 2.  Dendritic SNAREs add a new twist to the old neuron theory.

Authors:  Saak V Ovsepian; J Oliver Dolly
Journal:  Proc Natl Acad Sci U S A       Date:  2011-11-11       Impact factor: 11.205

Review 3.  SNARE requirements en route to exocytosis: from many to few.

Authors:  Ralf Mohrmann; Jakob B Sørensen
Journal:  J Mol Neurosci       Date:  2012-03-17       Impact factor: 3.444

4.  A coiled coil trigger site is essential for rapid binding of synaptobrevin to the SNARE acceptor complex.

Authors:  Katrin Wiederhold; Tobias H Kloepper; Alexander M Walter; Alexander Stein; Nickias Kienle; Jakob B Sørensen; Dirk Fasshauer
Journal:  J Biol Chem       Date:  2010-04-20       Impact factor: 5.157

Review 5.  The blockade of the neurotransmitter release apparatus by botulinum neurotoxins.

Authors:  Sergio Pantano; Cesare Montecucco
Journal:  Cell Mol Life Sci       Date:  2013-06-11       Impact factor: 9.261

6.  Lipid-anchored SNAREs lacking transmembrane regions fully support membrane fusion during neurotransmitter release.

Authors:  Peng Zhou; Taulant Bacaj; Xiaofei Yang; Zhiping P Pang; Thomas C Südhof
Journal:  Neuron       Date:  2013-10-10       Impact factor: 17.173

7.  PC12 cells that lack synaptotagmin I exhibit loss of a subpool of small dense core vesicles.

Authors:  Robert D Adams; Amy B Harkins
Journal:  Biophys J       Date:  2014-12-16       Impact factor: 4.033

Review 8.  Structure activity relationship of synaptic and junctional neurotransmission.

Authors:  Raj K Goyal; Arun Chaudhury
Journal:  Auton Neurosci       Date:  2013-03-25       Impact factor: 3.145

Review 9.  Molecular machines governing exocytosis of synaptic vesicles.

Authors:  Reinhard Jahn; Dirk Fasshauer
Journal:  Nature       Date:  2012-10-11       Impact factor: 49.962

10.  Analysis of SNARE complex/synaptotagmin-1 interactions by one-dimensional NMR spectroscopy.

Authors:  Amy Zhou; Kyle D Brewer; Josep Rizo
Journal:  Biochemistry       Date:  2013-05-07       Impact factor: 3.162

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